Full data view for gene GPR98


This database is one of the ”Retinal and hearing impairment genetic variant databases”. NOTE: gene symbol was recently changed from GPR98 to ADGRV1.
Information The variants shown are described using the NM_032119.3 transcript reference sequence.

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Paternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Proband M - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Paternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative M - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Paternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative F - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Paternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative F - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Paternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative F - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Maternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Proband M - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Maternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative M - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Maternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative F - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Maternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative F - Iran - - - - - 1 David Baux
+/+ 83i_85i c.17858-39959_18153-10974del r.(?) p.(Ile5953Valfs*42) Transmembrane 2 (5940-5960);Extracellular 1 (5961-5979);Transmembrane 3 (5980-6000);Cytoplasmic 2 (6001-6010);Transmembrane 4 (6011-6031);Extracellular 2 (6032-6059) Maternal (inferred) - pathogenic g.90221274_90357290del - 17857-39959_18153-10975del - GPR98_000005 homozygous Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Hilgert 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Hilgert 2009 Relative F - Iran - - - - - 1 David Baux
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